Electro-Mediated Redox Functionalization of Conjugated 1,3-Dienes Ophélie Montiège, Jean‐François Brière, Cédric Schneider, Hélène Beucher Advanced Synthesis and Catalysis, 2026 Conjugated 1,3‐dienes are abundant, readily available raw materials and key structural motifs in natural or bioactive molecules. The direct conversion of these versatile building blocks into value‐added products is an attractive area in synthetic chemistry. However, their selective functionalization remains a major challenge due to intrinsic regio‐ and stereoselectivity issues arising from multiple reactive sites. Traditional approaches, mostly involving two‐electron mediated transition‐metal catalysis, have faced challenges and motivated the development of new redox strategies, predominantly based on photocatalytic approaches. In this context, electrosynthesis has recently emerged as a competent and environmentally friendly alternative, allowing the generation of reactive metallic or open‐shelf organic radical intermediates under mild redox conditions. This comprehensive review provides an overview of electro‐mediated transformations of conjugated 1,3‐dienes, with an emphasis on the mechanisms involved. It is organized in three main sections encompassing hydrofunctionalization, two‐component difunctionalization and multicomponent processes.
Regio- and Stereoselective Electro-Mediated Carboalkoxylation of 1,3-Dienes Ophélie Montiège, Marion Siccardi, Morgane Sanselme, Cédric Schneider, Jean-François Brière, Hélène Beucher Organic Letters, 2024 1,3-Dienes are versatile raw materials for building molecular complexity. We report herein mild conditions for the regio- and stereoselective [only the ( E ) isomer obtained] 1,4-carboalkoxylation of 1,3-dienes. This electrochemical multicomponent reaction provides an eco-efficient and straightforward access to a diverse range of ( E )-polyfunctionalized allyl ether products, without requiring any metal catalyst.
Vinylogous and stereoselective domino synthesis of pyrano[2,3-c]pyrroles from alkylidene meldrum's acids Mariia Savchuk, Giang Vo-Thanh, Sylvain Oudeyer, Hélène Beucher, Jean-François Brière Organic and Biomolecular Chemistry, 2024 An expeditious diatereoselective synthesis of pyrano[2,3-c]pyrroles thanks to a domino Vinylogous aza-Michael-Aldol-Cyclocondensation (aza-VMAC) reaction to alkylidene Meldrum's acid derivatives.
An Organocatalytic and Stereoselective Vinylogous Domino Process towards Thiochromans Pierre Milbeo, Arthur Lebrêne, Mariia Savchuk, Giang Vo‐Thanh, Sylvain Oudeyer, Hélène Beucher, Jean‐François Brière Chemistry A European Journal, 2023 A highly diastereoselective organocatalyzed domino vinylogous sulfa‐Michael‐aldol‐cyclocondensation (VMAC) reaction has been developed using alkylidene Meldrum's acid as dienes highlighting two vinylogous steps, an unprecedented sulfa‐1,6‐conjugate addition and a diastereoselective aldol reaction triggering a formal (4+2) cycloaddition. This work opens a new route towards bio‐relevant and original tricyclic thiochroman derivatives.
Recent Advances in Catalytic and Technology-Driven Radical Addition to N,N-Disubstituted Iminium Species Sylvain Oudeyer, Vincent Levacher, Hélène Beucher, Jean-François Brière Molecules, 2023 Recently, radical chemistry has grown exponentially in the toolbox of organic synthetic chemists. Upon the (re)introduction of modern catalytic and technology-driven strategies, the implementation of highly reactive radical species is currently facilitated while expanding the scope of numerous synthetic methodologies. In this context, this review intends to cover the recent advances in radical-based transformations of N,N-disubstituted iminium substrates that encompass unique reactivities with respect to imines or protonated iminium salts. In particular, we have focused on the literature concerning the dipole type substrates, such as nitrones or azomethine imines, together with the chemistry of N+-X− (X = O, NR) azaarenium dipoles, which proved to be very versatile platforms in that field of research. The N-alkylazaarenium salts were been considered, which demonstrated specific reactivity profiles in radical chemistry.
Chelation-assisted C-C bond activation of biphenylene by gold(i) halides Hélène Beucher, Johannes Schörgenhumer, Estíbaliz Merino, Cristina Nevado Chemical Science, 2021 Pyridine and phosphine directing groups promote the C–C activation of biphenylene by readily available gold(i) halides rendering a new entry to (N^C^C)- and (P^C)-gold(iii) species.
Phosphorescent κ3-(N^C^C)-Gold(III) Complexes: Synthesis, Photophysics, Computational Studies and Application to Solution-Processable OLEDs Hélène Beucher, Sudhir Kumar, Roopender Kumar, Estíbaliz Merino, Wei‐Hsu Hu, Gerrit Stemmler, Sergio Cuesta‐Galisteo, Jorge A. González, Léonard Bezinge, Jakub Jagielski, Chih‐Jen Shih, Cristina Nevado Chemistry A European Journal, 2020 Efficient OLED devices have been fabricated using organometallic complexes of platinum group metals. Still, the high material cost and low stability represent central challenges for their application in commercial display technologies. Based on its innate stability, gold(III) complexes are emerging as promising candidates for high‐performance OLEDs. Here, a series of alkynyl‐, N‐heterocyclic carbene (NHC)‐ and aryl‐gold(III) complexes stabilized by a κ3‐(N^C^C) template have been prepared and their photophysical properties have been characterized in detail. These compounds exhibit good photoluminescence quantum efficiency (ηPL) of up to 33 %. The PL emission can be tuned from sky‐blue to yellowish green colors by variations on both the ancillary ligands as well as on the pincer template. Further, solution‐processable OLED devices based on some of these complexes display remarkable emissive properties (ηCE 46.6 cd.A−1 and ηext 14.0 %), thus showcasing the potential of these motifs for the low‐cost fabrication of display and illumination technologies.
Electro‐Mediated Redox Functionalization of Conjugated 1, 3‐Dienes O Montiège, JF Brière, C Schneider, H Beucher Advanced Synthesis & Catalysis 368 (6), e70362 , 2026 2026
Actes de la 9ème édition du colloque Pédagogie et Formation du Groupe INSA JP Kotowicz, N Delestre, V Hordey, N Matheu, H Paris, FS Touhami, ... Colloque Pédagogie et Formation du Groupe INSA, hal-05514577 , 2026 2026
Nickel-catalyzed direct cyanoalkylation of ketones. A Coffinet, J Yang, J Rio, M Savchuk, H Beucher, S Oudeyer, H Gérard, ... Journées de Chimie Organique (JCO 2025) , 2025 2025
Recent advances of asymmetric catalytic transformations of alkylidene Meldrum's acid derivatives H Beucher, V Levacher, S Oudeyer, JF Brière Chemical Communications 61 (36), 6555-6566 , 2025 2025 Citations: 3
Regio-and Stereoselective Electro-Mediated Carboalkoxylation of 1, 3-Dienes O Montiege, M Siccardi, M Sanselme, C Schneider, JF Brière, H Beucher Organic Letters 26 (51), 11105-11110 , 2024 2024 Citations: 2
Sels d’ammoniums quaternaires chiraux en organocatalyse: des outils polyvalents pour la synthèse asymétrique H Beucher, V Levacher, S Oudeyer, JF Brière L'Actualité Chimique 497, 23-25 , 2024 2024
Catalytic enantioselective synthesis of cyclopropyl α-amino carboxylates and phosphonates H Beucher, I Alahyen, A Talbot, T Poisson, P Jubault Organic Chemistry Frontiers 11 (20), 5859-5867 , 2024 2024 Citations: 4
Vinylogous and stereoselective domino synthesis of pyrano [2, 3-c] pyrroles from alkylidene meldrum's acids M Savchuk, G Vo-Thanh, S Oudeyer, H Beucher, JF Brière Organic & Biomolecular Chemistry 22 (15), 2948-2952 , 2024 2024 Citations: 1
Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light A Fall, M Magdei, M Savchuk, S Oudeyer, H Beucher, JF Brière Chemical Communications 60 (49), 6316-6319 , 2024 2024 Citations: 20
An Organocatalytic and Stereoselective Vinylogous Domino Process towards Thiochromans P Milbeo, A Lebrêne, M Savchuk, G Vo‐Thanh, S Oudeyer, H Beucher, ... Chemistry–A European Journal 29 (42), e202301311 , 2023 2023 Citations: 4
Recent Advances in Catalytic and Technology-Driven Radical Addition to N , N -Disubstituted Iminium Species S Oudeyer, V Levacher, H Beucher, JF Brière Molecules 28 (3), 1071 , 2023 2023 Citations: 15
Synthesis and Applications of Cyclometalated Gold (III) Complexes H Beucher University of Zurich , 2021 2021
Chelation-assisted C–C bond activation of biphenylene by gold (< scp> i</scp>) halides H Beucher, J Schörgenhumer, E Merino, C Nevado 2021
Chelation-assisted C–C bond activation of biphenylene by gold (I) halides H Beucher, J Schörgenhumer, E Merino, C Nevado Chemical Science 12 (45), 15084-15089 , 2021 2021 Citations: 12
Phosphorescent κ 3 ‐(N^C^C)‐Gold(III) Complexes: Synthesis, Photophysics, Computational Studies and Application to Solution‐Processable OLEDs H Beucher, S Kumar, R Kumar, E Merino, WH Hu, G Stemmler, ... Chemistry–A European Journal 26 (72), 17604-17612 , 2020 2020 Citations: 25
Highly Efficient Green Solution Processable Organic Light-Emitting Diodes Based on a Phosphorescent κ 3 -(N^C^C)Gold(III)-Alkynyl Complex H Beucher, S Kumar, E Merino, WH Hu, G Stemmler, S Cuesta-Galisteo, ... Chemistry of Materials 32 (4), 1605-1611 , 2020 2020 Citations: 46
Highly Efficient Green Solution Processable Organic Light-Emitting Diodes H Beucher, S Kumar, E Merino, WH Hu, G Stemmler, S Cuesta-Galisteo, ... 2020
κ 3 ‐(N^C^C)Gold(III) Carboxylates: Evidence for Decarbonylation Processes H Beucher, E Merino, A Genoux, T Fox, C Nevado Angewandte Chemie 131 (27), 9162-9165 , 2019 2019 Citations: 28
Minisci-photoredox-mediated α-heteroarylation of N-protected secondary amines: remarkable selectivity of azetidines C Bosset, H Beucher, G Bretel, E Pasquier, L Queguiner, C Henry, A Vos, ... Organic letters 20 (19), 6003-6006 , 2018 2018 Citations: 77
Rhodium-catalyzed cyclopropanation of fluorinated olefins: a straightforward route to highly functionalized fluorocyclopropanes A Pons, H Beucher, P Ivashkin, G Lemonnier, T Poisson, AB Charette, ... Organic Letters 17 (7), 1790-1793 , 2015 2015 Citations: 43
MOST CITED SCHOLAR PUBLICATIONS
Minisci-photoredox-mediated α-heteroarylation of N-protected secondary amines: remarkable selectivity of azetidines C Bosset, H Beucher, G Bretel, E Pasquier, L Queguiner, C Henry, A Vos, ... Organic letters 20 (19), 6003-6006 , 2018 2018 Citations: 77
Highly Efficient Green Solution Processable Organic Light-Emitting Diodes Based on a Phosphorescent κ 3 -(N^C^C)Gold(III)-Alkynyl Complex H Beucher, S Kumar, E Merino, WH Hu, G Stemmler, S Cuesta-Galisteo, ... Chemistry of Materials 32 (4), 1605-1611 , 2020 2020 Citations: 46
Rhodium-catalyzed cyclopropanation of fluorinated olefins: a straightforward route to highly functionalized fluorocyclopropanes A Pons, H Beucher, P Ivashkin, G Lemonnier, T Poisson, AB Charette, ... Organic Letters 17 (7), 1790-1793 , 2015 2015 Citations: 43
κ 3 ‐(N^C^C)Gold(III) Carboxylates: Evidence for Decarbonylation Processes H Beucher, E Merino, A Genoux, T Fox, C Nevado Angewandte Chemie 131 (27), 9162-9165 , 2019 2019 Citations: 28
Phosphorescent κ 3 ‐(N^C^C)‐Gold(III) Complexes: Synthesis, Photophysics, Computational Studies and Application to Solution‐Processable OLEDs H Beucher, S Kumar, R Kumar, E Merino, WH Hu, G Stemmler, ... Chemistry–A European Journal 26 (72), 17604-17612 , 2020 2020 Citations: 25
Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light A Fall, M Magdei, M Savchuk, S Oudeyer, H Beucher, JF Brière Chemical Communications 60 (49), 6316-6319 , 2024 2024 Citations: 20
Recent Advances in Catalytic and Technology-Driven Radical Addition to N , N -Disubstituted Iminium Species S Oudeyer, V Levacher, H Beucher, JF Brière Molecules 28 (3), 1071 , 2023 2023 Citations: 15
Chelation-assisted C–C bond activation of biphenylene by gold (I) halides H Beucher, J Schörgenhumer, E Merino, C Nevado Chemical Science 12 (45), 15084-15089 , 2021 2021 Citations: 12
Catalytic enantioselective synthesis of cyclopropyl α-amino carboxylates and phosphonates H Beucher, I Alahyen, A Talbot, T Poisson, P Jubault Organic Chemistry Frontiers 11 (20), 5859-5867 , 2024 2024 Citations: 4
An Organocatalytic and Stereoselective Vinylogous Domino Process towards Thiochromans P Milbeo, A Lebrêne, M Savchuk, G Vo‐Thanh, S Oudeyer, H Beucher, ... Chemistry–A European Journal 29 (42), e202301311 , 2023 2023 Citations: 4
Recent advances of asymmetric catalytic transformations of alkylidene Meldrum's acid derivatives H Beucher, V Levacher, S Oudeyer, JF Brière Chemical Communications 61 (36), 6555-6566 , 2025 2025 Citations: 3
Regio-and Stereoselective Electro-Mediated Carboalkoxylation of 1, 3-Dienes O Montiege, M Siccardi, M Sanselme, C Schneider, JF Brière, H Beucher Organic Letters 26 (51), 11105-11110 , 2024 2024 Citations: 2
Vinylogous and stereoselective domino synthesis of pyrano [2, 3-c] pyrroles from alkylidene meldrum's acids M Savchuk, G Vo-Thanh, S Oudeyer, H Beucher, JF Brière Organic & Biomolecular Chemistry 22 (15), 2948-2952 , 2024 2024 Citations: 1
Electro‐Mediated Redox Functionalization of Conjugated 1, 3‐Dienes O Montiège, JF Brière, C Schneider, H Beucher Advanced Synthesis & Catalysis 368 (6), e70362 , 2026 2026
Actes de la 9ème édition du colloque Pédagogie et Formation du Groupe INSA JP Kotowicz, N Delestre, V Hordey, N Matheu, H Paris, FS Touhami, ... Colloque Pédagogie et Formation du Groupe INSA, hal-05514577 , 2026 2026
Nickel-catalyzed direct cyanoalkylation of ketones. A Coffinet, J Yang, J Rio, M Savchuk, H Beucher, S Oudeyer, H Gérard, ... Journées de Chimie Organique (JCO 2025) , 2025 2025
Sels d’ammoniums quaternaires chiraux en organocatalyse: des outils polyvalents pour la synthèse asymétrique H Beucher, V Levacher, S Oudeyer, JF Brière L'Actualité Chimique 497, 23-25 , 2024 2024
Synthesis and Applications of Cyclometalated Gold (III) Complexes H Beucher University of Zurich , 2021 2021
Chelation-assisted C–C bond activation of biphenylene by gold (< scp> i</scp>) halides H Beucher, J Schörgenhumer, E Merino, C Nevado 2021
Highly Efficient Green Solution Processable Organic Light-Emitting Diodes H Beucher, S Kumar, E Merino, WH Hu, G Stemmler, S Cuesta-Galisteo, ... 2020